Variation in HTLV-I Sequences from Rabbit Cell Lines with Diverse in Vivo Effects
| Autor: | Tong Mao Zhao, Sansana Sawasdikosol, Thomas J. Kindt, R. Mark Simpson, Mary Ann Robinson |
|---|---|
| Rok vydání: | 1993 |
| Předmět: |
viruses
Molecular Sequence Data Biology Virus Cell Line Viral envelope In vivo hemic and lymphatic diseases Virology medicine Animals Humans chemistry.chemical_classification Human T-lymphotropic virus 1 Base Sequence Nucleic acid sequence Genetic Variation Provirus medicine.disease HTLV-I Infections Leukemia chemistry Cell culture DNA Viral Rabbits Glycoprotein |
| Zdroj: | Virology. 195:271-274 |
| ISSN: | 0042-6822 |
| Popis: | Comparison of nucleotide sequences determined for HTLV-I integrated provirus from two rabbit cell lines, RH/K30 and RH/K34, revealed greater than 99% identity to one another. Substitutions encoding amino acid interchanges were observed in the gag, pol, and rex regions whereas the env and tax proteins were identical in the two lines. Comparison with the human prototypic HTLV-I sequence revealed considerably more variation, especially in the vital envelope region where the rabbit sequences are identical. The HTLV-I lines differed in their potential to cause disease in rabbits: injection of the RH/K34 cell line caused human adult T-cell leukemia/lymphoma-like (ATLL) disease which was fatal within 10 days, whereas all rabbits injected with the same or higher doses of RH/K30 survived with a low-grade leukemia that showed evidence of acute rejection. Correlation of lethality with viral sequence was tested by injection of rabbits with two other rabbit cell lines with HTLV-I provirus identical to RH/K34 in LTR, gag, and env regions. The fact that only one of these lines produced fatal disease suggests that pathogenic determinants lie outside of these regions or, alternatively, that the structure of the integrated virus is not the sole factor in the cell lines' ability to cause ATLL-like disease. |
| Databáze: | OpenAIRE |
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